Global Trial Master File Quality Lead

Novartis Pharma Schweiz is seeking a Trial Master File Oversight Manager to lead the oversight of clinical trial documentation across a global portfolio. You will collaborate with cross-functional teams to ensure quality, integrity, and compliance, driving continuous improvement in TMF processes.

The ideal candidate will have a Bachelor's degree, at least five years of relevant experience in clinical research, and strong project management skills. Join us in transforming patient care through high-quality research.